ZNG1B Zn regulated GTPase metalloprotein activator 1B
Information
- Symbol
- ZNG1B
- Type
- protein-coding
- Description
- Zn regulated GTPase metalloprotein activator 1B
- Entrez Gene ID
- 150472
- Genome
- hg19
- Position
- chr2:114,195,268-114,253,781
- Genome
- hg38
- Position
- chr2:113,437,691-113,496,204
- MIM
- 611079 OMIM
- HGNC
- HGNC:17907 HGNC
- Ensembl
- ENSG00000136682 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
36 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CBWD2 |
MIM | 611079 OMIM |
HGNC | HGNC:17907 HGNC |
Ensembl | ENSG00000136682 Ensembl |
AllianceGenome | HGNC:17907 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000416503.6 | hg38 | chr2 | 113,437,763 | 113,496,171 | 58,409 |
ENST00000259199.9 | hg38 | chr2 | 113,437,691 | 113,496,204 | 58,514 |
ENST00000259199.9 | hg19 | chr2 | 114,195,268 | 114,253,781 | 58,514 |
ENST00000416503.6 | hg19 | chr2 | 114,195,340 | 114,253,748 | 58,409 |
Key | Value |
---|---|
strand | + |
start | 114,195,267 |
Gene Symbol | CBWD2 |
Entrez GeneId | 150,472 |
Chr Band | 2q13 |
end | 114,253,780 |
chr | chr2 |
Genome browser